3-phenylimidazolidine-2,4-dione-Imidazolidines| Ambeed

Chemistry Heterocyclic Building Blocks Imidazolidines 3-phenylimidazolidine-2,4-dione

3-phenylimidazolidine-2,4-dione

Ambeed provide 4 derivatives of 3-phenylimidazolidine-2,4-dione.

These compounds have the same murcko framework: 3-phenylimidazolidine-2,4-dione.

Acid-Base Reactions: Phenytoin contains an imidazole ring, which can act as a weak base. It can react with strong acids to form salts. For example, it can react with hydrochloric acid to form phenytoin hydrochloride.
Oxidation: Phenytoin can undergo oxidation reactions. In the body, it is metabolized by hepatic enzymes, primarily by the cytochrome P450 system. The oxidation products include 5-(4-hydroxyphenyl)-5-phenylhydantoin and 5-(4,4-dihydroxyphenyl)-5-phenylhydantoin.
Reduction: Phenytoin can undergo reduction reactions under certain conditions. This can lead to the formation of different reduced products.
Nucleophilic Substitution: The carbonyl group in the imidazolidine-2,4-dione ring is susceptible to nucleophilic attack. This can occur in reactions with strong nucleophiles.
Esterification: The carboxyl group in the structure can potentially react in esterification reactions with alcohols and a suitable catalyst.
Photochemical Reactions: Like many organic compounds, phenytoin can undergo photochemical reactions when exposed to ultraviolet (UV) light.
Metal Complexation: Phenytoin can form complexes with various metal ions, particularly transition metals.
Decomposition Reactions: When subjected to high temperatures or extreme conditions, phenytoin may undergo decomposition reactions.

3-phenylimidazolidine-2,4-dione

A108339154992-24-298%

$17.00/100mg

A24221463612-50-099%

$261.00/5g

A1709952221-13-895%

$394.00/5g

A256531143782-20-195%

$203.00/1g